ENST00000255078.8:c.1774G>T
MANE Select
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ENSP00000255078.4:p.Ala592Ser
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ENST00000674675.1:c.18G>T
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ENST00000674878.1:c.18G>T
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ENST00000674955.1:c.*491G>T
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ENSP00000502463.1:n.*491G>T
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ENST00000675118.1:c.1262G>T
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ENST00000675389.1:n.49G>T
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ENST00000675615.1:c.1774G>T
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ENSP00000502413.1:p.Ala592Ser
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ENST00000675648.1:n.1149G>T
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ENST00000675916.1:c.18G>T
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ENST00000676173.1:n.2519G>T
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ENST00000676182.1:c.205G>T
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ENST00000676228.1:c.*1097G>T
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ENSP00000502375.1:n.*1097G>T
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ENST00000255078.7:c.1774G>T
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ENSP00000255078.3:p.Ala592Ser
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ENST00000539064.5:n.1533G>T
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ENST00000541229.5:n.469G>T
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ENST00000543739.5:n.767G>T
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ENST00000545475.1:n.370G>T
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NM_002180.2:c.1774G>T , LRG_250t1:c.1774G>T
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NP_002171.2:p.Ala592Ser
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XM_005273974.2:c.763G>T
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XP_005274031.1:p.Ala255Ser
|
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XM_005273975.2:c.646G>T
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XP_005274032.1:p.Ala216Ser
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XM_011544994.1:c.541G>T
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XP_011543296.1:p.Ala181Ser
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XR_949903.1:n.1876G>T
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XM_005273975.3:c.646G>T
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XP_005274032.1:p.Ala216Ser
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XM_017017669.2:c.763G>T
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XP_016873158.1:p.Ala255Ser
|
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XM_017017670.2:c.763G>T
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XP_016873159.1:p.Ala255Ser
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XR_949903.3:n.1872G>T
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NM_002180.3:c.1774G>T
MANE Select
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NP_002171.2:p.Ala592Ser
|
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